- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Aug 14, 2026
03108665004GR4 references
03108665004GRNo device characteristics flagged
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
Q010204Retraction wires and gingival retractors4 references
| Product | Trade name | Reference / catalog number | Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary → | Quantity | Status |
|---|---|---|---|---|---|
| Retrax Gel AS Clear Pro Pack | Retrax Gel AS Clear Pro Pack | 16840 | 00310866002330 | 1 | On the market |
| Retrax Gel FS 30g Jar | Retrax Gel FS 30g Jar | 15710 | 00310866002354 | 1 | On the market |
| Retrax Gel FS 30g Jar | Retrax Gel FS 30g Jar | 15710 | 00310866000909 | 1 | On the market |
| Retrax Gel FS Pro Pack | Retrax Gel FS Pro Pack | 16740 | 00310866002323 | 1 | On the market |